Interaction of stromal and microvascular components in keratocystic odontogenic tumors

Objective Little is known about the interaction of stromal components in odontogenic tumors. Thus, the aim of this study was to investigate mast cells (MCs), myofibroblasts, macrophages, and their possible association with angiogenesis and lymphangiogenesis in keratocystic odontogenic tumors (KCOTs)...

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Veröffentlicht in:Journal of oral pathology & medicine 2016-09, Vol.45 (8), p.557-564
Hauptverfasser: Sousa-Neto, Ernesto Santos, Cangussu, Maria Cristina Teixeira, Gurgel, Clarissa Araújo, Guimarães, Vanessa Sousa, Ramos, Eduardo Antônio Gonçalves, Xavier, Flávia Caló Aquino, Cury, Patrícia Ramos, Carneiro Júnior, Braúlio, Leonardi, Rosalia, Dos Santos, Jean Nunes
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Sprache:eng
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Zusammenfassung:Objective Little is known about the interaction of stromal components in odontogenic tumors. Thus, the aim of this study was to investigate mast cells (MCs), myofibroblasts, macrophages, and their possible association with angiogenesis and lymphangiogenesis in keratocystic odontogenic tumors (KCOTs). Material and Methods Thirty cases of KCOTs were included and analyzed by immunohistochemistry for mast cell tryptase, α‐SMA, CD34, CD163, and D240. For comparative purpose, 15 radicular cysts (CRs) and 7 pericoronal follicles (PFs) were included. Results There was an increase in MCs for RCs and this difference was significant when they were compared to KCOTS and PFs. A significant increase in the density of MFs was observed for KCOTs when compared to RCs and PFs (P = 0.00). No significant difference in CD163‐positive macrophages (P = 0.084) and CD34‐positive vessels (P = 0.244) densities was observed between KCOTs, RCs, and PFs, although KCOTs showed a higher density of all proteins. Significant difference in lymphatic vessel density was observed for KCOTs when compared to RCs and PFs (P = 0.00). Positive correlation was observed between mast cell tryptase and CD34 in KCOTs (P = 0.025). Conclusions A significant interaction between the MC population and CD34‐positive vessels in KCOTs supported the hypothesis that MCs and blood vessels contribute to the stromal scaffold of KCOT.
ISSN:0904-2512
1600-0714
DOI:10.1111/jop.12400